IP Library Granted Patent US 9,587,061
Granted Patent B2
US 9,587,061 · App. 14/973,235 · Granted Mar 7, 2017

Co-crosslinker systems for encapsulation films comprising urea compounds

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Quick Facts
Patent No.
US 9,587,061
App. No.
14/973,235
Granted
Mar 7, 2017
Kind
B2
Abstract

A first composition (A) contains (i) at least one compound (I) selected from the group consisting of triallyl isocyanurate, and triallyl cyanurate, wherein the compound (I) is preferably triallyl isocyanurate; and (ii) at least one urea compound. A second composition (B) contains the first composition (A) and at least one polyolefin copolymer. Composition (B) is used for producing a film for encapsulating an electronic device, in particular a solar cell.

Claims (41)

1. A composition (A), comprising:

(i) at least one compound (I) selected from the group consisting of triallyl isocyanurate, and triallyl cyanurate; and

(ii) at least one compound (II);

wherein the compound (II) is defined by a chemical structural formula selected from the group consisting of (II-A), (II-B), (II-C), (II-D) wherein

and wherein

n=0 or 1;

A 1 , A 2 , A 3 , A 4 , A 5 , A 6 , A 7 , A 8 are each independently of one another selected from the group consisting of i) a methacryloyl group, ii) an acryloyl group, and iii) a branched or unbranched alkenyl group having 3 to 18 carbon atoms and having at least one terminal double bond;

R 1 , R 2 , R 3 , R 4 , R 5 are each independently of one another selected from the group consisting of the following a, b and c):

a) hydrogen,

b) a branched or unbranched alkyl group having 1 to 20 carbon atoms, wherein one or more hydrogen radicals may each be substituted by a halogen radical and wherein in addition one or two hydrogen radicals may each be substituted by a radical selected from the group consisting of —OR 6 , and —C(═O)NR 7 R 8 , wherein R 6 , R 7 , R 8 are each independently of one another selected from the group consisting of hydrogen, branched and unbranched alkyl group having 1 to 10 carbon atoms, and

c) a cycloalkyl group having 3 to 12 carbon atoms, wherein one or more hydrogen radicals may each be substituted by a halogen radical and wherein in addition one or two hydrogen radicals may each be substituted by a radical selected from the group consisting of —OR 9 , and —C(═O)NR 10 R 11 , wherein R 9 , R 10 , R 11 are each independently of one another selected from the group consisting of hydrogen, and a branched and unbranched alkyl group having 1 to 10 carbon atoms,

and wherein the radicals R 1 and R 2 may each also be selected from the group consisting of methacryloyl group, acryloyl group, and a branched or unbranched alkenyl group having 3 to 18 carbon atoms and having at least one terminal double bond;

and wherein at least one compound (II) in the composition (A) is present in a proportion of at least 1% by weight based on a total weight of all compounds (I) in the composition (A).

2. The composition (A) according to claim 1 , wherein the compound (I) is triallyl isocyanurate.

3. The composition (A) according to claim 1 , wherein n=0 or 1;

A 1 , A 2 , A 3 , A 4 , A 5 , A 6 , A 7 , A 8 are each independently of one another selected from the group consisting of a methacryloyl group, an acryloyl group, and an allyl group;

R 1 , R 2 , R 3 , R 4 , R 5 are each independently of one another selected from the group consisting of hydrogen, and a branched or unbranched alkyl group having 1 to 20 carbon atoms;

and wherein in addition the radicals R 1 and R 2 may each also be selected from the group consisting of a methacryloyl group, an acryloyl group, and an allyl group.

4. The composition (A) according to claim 3 , wherein the compound (II) is defined by a chemical structural formula selected from the group consisting of (II-A), and (II-B);

and wherein

A 1 , A 2 , A 3 , A 4 are each independently of one another selected from the group consisting of a methacryloyl group, an acryloyl group, and an allyl group;

R 1 , R 2 , R 3 , R 4 are each independently of one another selected from the group consisting of hydrogen, and a branched or unbranched alkyl group having 1 to 20 carbon atoms;

and wherein in addition the radicals R 1 and R 2 may each also be selected from the group consisting of a methacryloyl group, an acryloyl group, and an allyl group.

5. The composition (A) according to claim 1 , wherein a total weight of all compounds (II) in the composition (A) is 1% to 50% by weight based on a total weight of all compounds (I) in the composition (A).

6. The composition (B), comprising:

at least one polyolefin copolymer; and

a composition (A) according to claim 1 .

7. The composition (B) according to claim 6 , wherein the polyolefin copolymer is an ethylene-vinyl acetate copolymer.

8. The composition (B) according to claim 7 , wherein the ethylene-vinyl acetate copolymer has a vinyl acetate content of 15% to 50% by weight based on a total weight of the ethylene-vinyl acetate copolymer and determined as per ASTM D 5594:1998.

9. The composition (B) according to claim 6 , in which the proportion of composition (A) is 0.05% to 10% by weight based on a mass of all polyolefin copolymers in the composition (B).

10. The composition (B) according to claim 6 which further comprises at least one initiator selected from the group consisting of peroxidic compounds, azo compounds, and photo initiators.

11. The composition (B) according to claim 10 , wherein the initiator is a peroxidic compound.

12. The composition (B) according to claim 6 which further comprises at least one compound (D) selected from the group consisting of crosslinkers, silane coupling agents, antioxidants, ageing stabilizers, metal oxides, metal hydroxides, and white pigments.

13. The composition (B) according to claim 12 , wherein the compound (D) is a silane coupling agent.

14. A film for encapsulation of an electronic device, comprising:

the composition (B) according to claim 6 in crosslinked form.

15. The film according to claim 14 , wherein the device is a solar cell.

16. A method for encapsulating an electronic device, comprising:

contacting said electronic device with the composition (B) of claim 6 and crosslinking said composition (B).

17. The method according to claim 16 , wherein the device is a solar cell.

18. The method according to claim 17 , wherein the crosslinking of the composition (B) occurs in the course of solar module lamination.

Assignments (3)
CONFIRMATORY ASSIGNMENT Recorded Mar 21, 2023
From: EVONIK OPERATIONS GMBH
To: EVONIK CYC GMBH
Reel/Frame 063123/0028 →
CHANGE OF NAME Recorded Jan 31, 2020
From: EVONIK DEGUSSA GMBH
To: EVONIK OPERATIONS GMBH
Reel/Frame 051765/0166 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 7, 2016
From: ULBRICHT, DANIEL; HEIN, MARCEL; KLEFF, FRANK; SCHAUHOFF, STEPHANIE; OHLEMACHER, JUERGEN
To: EVONIK DEGUSSA GMBH
Reel/Frame 037901/0816 →